Sunpharma
bullish highSun Pharma delivered a strong Q2 FY25 with consolidated sales of INR 13,264 crore, up 10.5% YoY, driven by US specialty growth (+20.3% to $517M) and India formulation growth (+11%).
Read Sunpharma analysis →Side-by-side earnings comparison across financial stats, AI summaries, management guidance, risks, quotes, and accountability signals.
Sun Pharma delivered a strong Q2 FY25 with consolidated sales of INR 13,264 crore, up 10.5% YoY, driven by US specialty growth (+20.3% to $517M) and India formulation growth (+11%).
Read Sunpharma analysis →Cipla reported Q2 FY25 revenue of INR 7,051 crore (+9% YoY) and an EBITDA margin of 26.7% (highest ever, +70bps YoY), driven by strong profitability in India chronic therapies and Africa growth.
Read Cipla analysis →Sun Pharma delivered a strong Q2 FY25 with consolidated sales of INR 13,264 crore, up 10.5% YoY, driven by US specialty growth (+20.3% to $517M) and India formulation growth (+11%). EBITDA margin expanded 350 bps YoY to 29.6%, aided by favorable product mix and lower material costs. PAT grew 28% YoY to INR 3,040 crore. The US specialty portfolio (Ilumya, Winlevi, Cequa) continues to perform well, while the India business gained market share to 8.1%. R&D spend guidance was revised down to 7-8% of sales due to clinical trial delays. Key risks include the binary outcome of Leqselvi patent litigation and potential margin pressure from higher selling expenses.
Cipla reported Q2 FY25 revenue of INR 7,051 crore (+9% YoY) and an EBITDA margin of 26.7% (highest ever, +70bps YoY), driven by strong profitability in India chronic therapies and Africa growth. PAT stood at INR 1,303 crore (18.5% of sales). One India grew 5% YoY, impacted by weak acute season, but chronic therapies outpaced market. North America revenue was $237 million, with lanreotide franchise at 35% market share but facing supply issues expected to resolve by Q4. Africa grew 22% with South Africa private market ranking #2. Management maintained EBITDA margin guidance of 24.5%-25.5% for FY25. Key risks include lanreotide supply disruption, Goa FDA classification uncertainty, and potential pricing erosion in US generics.
US business grew 20.3% YoY to $517M, driven by specialty portfolio and lenalidomide.
Sun Pharma's market share in the Indian pharma market increased to 8.1% from 7.7%.
Global specialty sales grew 19.2% YoY to $286M, led by Ilumya and other key brands.
Sun's volume growth in India was 5.2% vs IPM's 0.7%, driven by new launches and field force expansion.
Combined 505(b)(2) and ANDA assets reached 35% share in Q2, but supply issues will reduce Q3 sales.
Share of chronic therapies in India branded prescription business improved to 61.5% as per IQVIA.
Ibudilast further enhanced its market share to 19% in Q2.
Overall US portfolio price erosion of about 10% year-on-year, with QoQ low single digits.
R&D spend for FY25 is expected to be in the range of 7-8% of sales, down from earlier guidance of 8-10%, due to delays in clinical studies.
Management guidance growthManagement stated they would be ready to launch Leqselvi within a couple of weeks post a favorable court ruling on the patent litigation.
Management guidance otherPhase III data for Ilumya in psoriatic arthritis is expected in the second half of calendar year 2025, with launch shortly after approval.
Management guidance growthManagement reiterated full-year EBITDA margin guidance despite Q2 margin of 26.7%, expecting normalized Q3 and Q4.
Management guidance marginsRisking of generic Advair progressing as per expectations; launch targeted for first half of fiscal 2026.
Management guidance growthSupply challenges expected to be resolved by end of Q3, with sharp recovery in lanreotide franchise from Q4 FY25.
Management guidance otherManagement expects India business to revert to growth trajectory with respiratory uptick in Q3 and outpace market growth for the full year.
Management guidance growthThe Leqselvi launch depends on a favorable court ruling on the '335 patent; an unfavorable outcome could delay launch until patent expiry in Dec 2026.
high · analyst_questionManagement acknowledged that further delays in clinical trials could keep R&D spend below the revised 7-8% guidance.
medium · management_commentaryOther expenses rose significantly due to higher selling and distribution costs in US and EM, which could pressure margins if not offset by revenue growth.
medium · data_observationPrice cuts in Japan are expected to continue pressuring ROW revenues for the next few quarters, as mentioned by management.
medium · management_commentarySupply issues at partner site will reduce Q3 lanreotide sales significantly; recovery depends on partner's production ramp-up.
high · management_commentaryGoa facility received Form 483 observations; classification still awaited, which could impact Abraxane launch timeline and other approvals.
high · management_commentaryBlended US price erosion of ~10% YoY, with potential for further pressure from new competition in Albuterol and other products.
medium · analyst_questionSlow seasonal growth in acute category, especially anti-infectives, impacted India business; recovery dependent on respiratory season.
medium · data_observationOur focus was on generating a more profitable prescription. I think we've been able to achieve that.
We are very excited. Only issue is how fast can we bring the product to market, and what kind of clinical outcome benefit we are able to show while the product is in registration.
This quarter, we yet again delivered a strong profitability. The reported EBITDA margin stood at 26.7% for the quarter, which is the highest ever quarterly EBITDA margin that's reported by Cipla.
In lanreotide, we are in the process of resolving our supply issues. Our trade generics business, the model change has been successfully implemented, and we now have a better control on the channel.